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Effect of montelukast on platelet activating factor- and tachykinin induced mucus secretion in the rat

BACKGROUND: Platelet activating factor and tachykinins (substance P, neurokinin A, neurokinin B) are important mediators contributing to increased airway secretion in the context of different types of respiratory diseases including acute and chronic asthma. Leukotriene receptor antagonists are recom...

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Autores principales: Schmidt, Rene, Staats, Petra, Groneberg, David A, Wagner, Ulrich
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2278150/
https://www.ncbi.nlm.nih.gov/pubmed/18289370
http://dx.doi.org/10.1186/1745-6673-3-5
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author Schmidt, Rene
Staats, Petra
Groneberg, David A
Wagner, Ulrich
author_facet Schmidt, Rene
Staats, Petra
Groneberg, David A
Wagner, Ulrich
author_sort Schmidt, Rene
collection PubMed
description BACKGROUND: Platelet activating factor and tachykinins (substance P, neurokinin A, neurokinin B) are important mediators contributing to increased airway secretion in the context of different types of respiratory diseases including acute and chronic asthma. Leukotriene receptor antagonists are recommended as add-on therapy for this disease. The cys-leukotriene-1 receptor antagonist montelukast has been used in clinical asthma therapy during the last years. Besides its inhibitory action on bronchoconstriction, only little is known about its effects on airway secretions. Therefore, the aim of this study was to evaluate the effects of montelukast on platelet activating factor- and tachykinin induced tracheal secretory activity. METHODS: The effects of montelukast on platelet activating factor- and tachykinin induced tracheal secretory activity in the rat were assessed by quantification of secreted (35)SO(4 )labelled mucus macromolecules using the modified Ussing chamber technique. RESULTS: Platelet activating factor potently stimulated airway secretion, which was completely inhibited by the platelet activating factor receptor antagonist WEB 2086 and montelukast. In contrast, montelukast had no effect on tachykinin induced tracheal secretory activity. CONCLUSION: Cys-leukotriene-1 receptor antagonism by montelukast reverses the secretagogue properties of platelet activating factor to the same degree as the specific platelet activating factor antagonist WEB 2086 but has no influence on treacheal secretion elicited by tachykinins. These results suggest a role of montelukast in the signal transduction pathway of platelet activating factor induced secretory activity of the airways and may further explain the beneficial properties of cys-leukotriene-1 receptor antagonists.
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spelling pubmed-22781502008-04-02 Effect of montelukast on platelet activating factor- and tachykinin induced mucus secretion in the rat Schmidt, Rene Staats, Petra Groneberg, David A Wagner, Ulrich J Occup Med Toxicol Research BACKGROUND: Platelet activating factor and tachykinins (substance P, neurokinin A, neurokinin B) are important mediators contributing to increased airway secretion in the context of different types of respiratory diseases including acute and chronic asthma. Leukotriene receptor antagonists are recommended as add-on therapy for this disease. The cys-leukotriene-1 receptor antagonist montelukast has been used in clinical asthma therapy during the last years. Besides its inhibitory action on bronchoconstriction, only little is known about its effects on airway secretions. Therefore, the aim of this study was to evaluate the effects of montelukast on platelet activating factor- and tachykinin induced tracheal secretory activity. METHODS: The effects of montelukast on platelet activating factor- and tachykinin induced tracheal secretory activity in the rat were assessed by quantification of secreted (35)SO(4 )labelled mucus macromolecules using the modified Ussing chamber technique. RESULTS: Platelet activating factor potently stimulated airway secretion, which was completely inhibited by the platelet activating factor receptor antagonist WEB 2086 and montelukast. In contrast, montelukast had no effect on tachykinin induced tracheal secretory activity. CONCLUSION: Cys-leukotriene-1 receptor antagonism by montelukast reverses the secretagogue properties of platelet activating factor to the same degree as the specific platelet activating factor antagonist WEB 2086 but has no influence on treacheal secretion elicited by tachykinins. These results suggest a role of montelukast in the signal transduction pathway of platelet activating factor induced secretory activity of the airways and may further explain the beneficial properties of cys-leukotriene-1 receptor antagonists. BioMed Central 2008-02-20 /pmc/articles/PMC2278150/ /pubmed/18289370 http://dx.doi.org/10.1186/1745-6673-3-5 Text en Copyright © 2008 Schmidt et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Schmidt, Rene
Staats, Petra
Groneberg, David A
Wagner, Ulrich
Effect of montelukast on platelet activating factor- and tachykinin induced mucus secretion in the rat
title Effect of montelukast on platelet activating factor- and tachykinin induced mucus secretion in the rat
title_full Effect of montelukast on platelet activating factor- and tachykinin induced mucus secretion in the rat
title_fullStr Effect of montelukast on platelet activating factor- and tachykinin induced mucus secretion in the rat
title_full_unstemmed Effect of montelukast on platelet activating factor- and tachykinin induced mucus secretion in the rat
title_short Effect of montelukast on platelet activating factor- and tachykinin induced mucus secretion in the rat
title_sort effect of montelukast on platelet activating factor- and tachykinin induced mucus secretion in the rat
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2278150/
https://www.ncbi.nlm.nih.gov/pubmed/18289370
http://dx.doi.org/10.1186/1745-6673-3-5
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